Publications by authors named "Katrina Harrison"

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De Novo GLI2 Missense Variant in a Child With Isolated Hypopituitarism and Craniofacial Anomalies: Expanding the Phenotypic Spectrum.
Himanshu Goel, Katrina Harrison

Mol Genet Genomic Med· September 2025

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Nationwide, Couple-Based Genetic Carrier Screening.
Edwin P Kirk, Martin B Delatycki, Alison D Archibald, Erin Tutty, Jade Caruana, Katrina Harrison

N Engl J Med· November 2024

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Identification of clinically actionable variants from genome sequencing of families with congenital heart disease.
Dimuthu Alankarage, Eddie Ip, Justin O Szot, Jacob Munro, Gillian M Blue, Katrina Harrison

Genet Med· May 2019

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A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data.
Justin O Szot, Hartmut Cuny, Gillian M Blue, David T Humphreys, Eddie Ip, Katrina Harrison

Circ Genom Precis Med· March 2018

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Clinical significance of circulating microRNAs as markers in detecting and predicting congenital heart defects in children.
Yong Song, Hilda Higgins, Jing Guo, Katrina Harrison, En Nee Schultz

J Transl Med· February 2018

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Compliance with professional guidelines with reference to familial cancer services.
Gaenor Kyne, Susannah Maxwell, Kate Brameld, Katrina Harrison, Jack Goldblatt

Aust N Z J Public Health· June 2011

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